Organic Letters, volume 7, issue 25, pages 5725-5727
Abnormally mild synthesis of bis(dithiolo)pyrroles from 2,5-dimethylpyrroles
Publication type: Journal Article
Publication date: 2005-11-17
Journal:
Organic Letters
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.2
ISSN: 15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
[chemical reaction: see text]. Treatment of N-substituted 2,5-dimethylpyrroles 2 with an equilibrated mixture of disulfur dichloride and DABCO in chloroform at 0 degrees C gives pentathiepinopyrroles 3 in moderate yields; further reaction of 3 with the same mixture at room temperature leads, in an extensive reaction cascade, to bis(dithiolo)pyrroles 4 in high yield; 2 can be converted into 4 in a one-pot operation under unusually mild conditions.
Citations by journals
1
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Russian Chemical Reviews
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1 publication, 4.55%
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Tetrahedron
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Advances in Heterocyclic Chemistry
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1 publication, 4.55%
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Russian Chemical Bulletin
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1 publication, 4.55%
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Mendeleev Communications
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1 publication, 4.55%
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Molecules
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Molecules
1 publication, 4.55%
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ChemInform
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1 publication, 4.55%
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Journal of Organic Chemistry
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1 publication, 4.55%
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Angewandte Chemie
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Angewandte Chemie
1 publication, 4.55%
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Angewandte Chemie - International Edition
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Angewandte Chemie - International Edition
1 publication, 4.55%
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Organic Letters
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1 publication, 4.55%
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Progress in Heterocyclic Chemistry
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1 publication, 4.55%
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Synlett
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Synlett
1 publication, 4.55%
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1
2
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Citations by publishers
1
2
3
4
5
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Elsevier
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Elsevier
5 publications, 22.73%
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Wiley
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Wiley
4 publications, 18.18%
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Multidisciplinary Digital Publishing Institute (MDPI)
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Multidisciplinary Digital Publishing Institute (MDPI)
2 publications, 9.09%
|
Springer Nature
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Springer Nature
2 publications, 9.09%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
2 publications, 9.09%
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American Chemical Society (ACS)
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American Chemical Society (ACS)
2 publications, 9.09%
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Thieme
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Thieme
1 publication, 4.55%
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1
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3
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5
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- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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Amelichev S. A. et al. Abnormally mild synthesis of bis(dithiolo)pyrroles from 2,5-dimethylpyrroles // Organic Letters. 2005. Vol. 7. No. 25. pp. 5725-5727.
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Amelichev S. A., Aysin R., Konstantinova L. S., Obruchnikova N. V., Rakitin O. A., Rees C. W. Abnormally mild synthesis of bis(dithiolo)pyrroles from 2,5-dimethylpyrroles // Organic Letters. 2005. Vol. 7. No. 25. pp. 5725-5727.
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TY - JOUR
DO - 10.1021/ol052557v
UR - https://doi.org/10.1021%2Fol052557v
TI - Abnormally mild synthesis of bis(dithiolo)pyrroles from 2,5-dimethylpyrroles
T2 - Organic Letters
AU - Amelichev, Stanislav A.
AU - Konstantinova, Lidia S.
AU - Obruchnikova, Natalia V.
AU - Rees, Charles W.
AU - Aysin, Rinat
AU - Rakitin, Oleg A.
PY - 2005
DA - 2005/11/17 00:00:00
PB - American Chemical Society (ACS)
SP - 5725-5727
IS - 25
VL - 7
SN - 1523-7060
SN - 1523-7052
ER -
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@article{2005_Amelichev,
author = {Stanislav A. Amelichev and Lidia S. Konstantinova and Natalia V. Obruchnikova and Charles W. Rees and Rinat Aysin and Oleg A. Rakitin},
title = {Abnormally mild synthesis of bis(dithiolo)pyrroles from 2,5-dimethylpyrroles},
journal = {Organic Letters},
year = {2005},
volume = {7},
publisher = {American Chemical Society (ACS)},
month = {nov},
url = {https://doi.org/10.1021%2Fol052557v},
number = {25},
pages = {5725--5727},
doi = {10.1021/ol052557v}
}
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MLA
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Amelichev, Stanislav A., et al. “Abnormally mild synthesis of bis(dithiolo)pyrroles from 2,5-dimethylpyrroles.” Organic Letters, vol. 7, no. 25, Nov. 2005, pp. 5725-5727. https://doi.org/10.1021%2Fol052557v.